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The protein encoded by CRTAP is similar to the chicken and mouse CRTAP genes. Additionally we are shipping CRTAP Kits (15) and CRTAP Proteins (11) and many more products for this protein.
Showing 10 out of 71 products:
Human Monoclonal CRTAP Primary Antibody for IHC (p), ELISA - ABIN564572
Chang, Barnes, Cabral, Bodurtha, Marini: Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex. in Human molecular genetics 2009
Show all 3 Pubmed References
To the best of our knowledge, our study is the first to exclude potential correlations between heterozygous variants in CRTAP and milder skeletal impairments in a large number of patients
This study enhances our knowledge about the mutational pattern of the LEPRE1 (show LEPRE1 Antibodies), CRTAP, and PPIB (show PPIB Antibodies) genes. LEPRE1 (show LEPRE1 Antibodies) should be the first gene analyzed in mutation detection studies in patients with recessive OI.
An additional function of the rough endoplasmic reticulum protein complex prolyl 3-hydroxylase 1.cartilage-associated protein.cyclophilin B: the CXXXC motif reveals disulfide isomerase activity in vitro.
SNP rs7623768 and the haplotype G-C of rs4076086-rs7623768 in CRTAP were associated with femoral neck bone mineral density (p = 0.009 and p = 0.003, respectively).
Importantly, human mutations in the CRTAP gene have been associated with recessive forms of OI.
CRTAP deficiency results in higher bone mineral content of the bone matrix in osteogenesis imperfecta type VII.
Null mutations in LEPRE1 (show LEPRE1 Antibodies) and CRTAP cause severe recessive osteogenesis imperfecta (show COL1A2 Antibodies).
CRTAP and P3H1 (show LEPRE1 Antibodies) are mutually stabilized in the collagen prolyl 3-hydroxylation complex in endoplasmic reticulum.
CRTAP mutations not described earlier were identified in 10 individuals who had a clinical diagnosis of lethal and severe osteogenesis imperfecta (show COL1A2 Antibodies).
complexes with prolyl 3-hydroxylase 1 (P3H1) to decrease prolyl 3 hydroxylation; dysregulation (show COL1A2 Antibodies) of prolyl 3 hydroxylation is a (show TH Antibodies) mechanism for connective tissue disease
This substitution abolished P3h1 (show LEPRE1 Antibodies) activity but retained ability to form a complex with Crtap and thus the collagen chaperone function.
In Crtap-deficient mice, the mineral content of the bone matrix is abnormally high; there are increased mineral densities at all measured sites for murine femora compared to control animals.
CRTAP mutations are associated with the clinical spectrum of recessive osteogenesis imperfecta (show COL1A2 Antibodies), including the type II and VII (show TH Antibodies) forms
The protein encoded by this gene is similar to the chicken and mouse CRTAP genes. The encoded protein is a scaffolding protein that may influence the activity of at least one member of the cytohesin/ARNO family in response to specific cellular stimuli. Defects in this gene are associated with osteogenesis imperfecta, a connective tissue disorder characterized by bone fragility and low bone mass.
, cartilage associated protein
, leprecan-like 3